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SELECTBIO Conferences Cancer Immunotherapy & Biofluid Biopsies 2016

David Fabrizio's Biography



David Fabrizio, Leader, Cancer Immunotherapy, Foundation Medicine

Leader, Cancer Immunotherapy
Foundation Medicine, Inc.
Cambridge, MA

David Fabrizio has over 12 years of experience in the drug discovery industry, and more recently in the application of next generation sequencing technologies to discover methods for cancer immunotherapy response. David’s early work helped lead to the discovery of a novel BMP signaling molecule, RGMb (DRAGON), which was later discovered to be a receptor for the immune checkpoint PDL2, and was published in the Journal of Biochemistry in 2005. David joined Adnexus Therapeutics in 2004, and went on to develop novel checkpoint inhibitor immunotherapies, helping to lead the PD1/PDL1 pre-clinical drug discovery effort which was eventually acquired by Bristol Myers Squibb in 2007. Additionally, his work lead to several issued patents, including for those describing novel EGFR and IGFR targeting therapeutics, as well as a method for improved drug pharmacokinetics through novel human serum albumin binding motifs. While at BMS, David also invented a novel drug selection technology, ASCENT, to rapidly identify protein based therapeutic binders using a reconstituted mRNA/protein fusion system. In 2013, David joined the startup, AbVitro, and focused on developing an NGS immune cell sequencing/antigen target identification technology, which was recently acquired by Juno Therapeutics. David joined Foundation medicine in 2015, and currently leads the Cancer Immunotherapy group, which is utilizing NGS techniques to identify methods for the identification of responders to immunotherapies, including checkpoint inhibitors.

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Tumor Mutational Burden as a Biomarker for Immunotherapy – Clinical Feasibility in NSCLC, Melanoma and Advanced Urothelial Carcinoma

Wednesday, 2 November 2016 at 13:30

Add to Calendar ▼2016-11-02 13:30:002016-11-02 14:30:00Europe/LondonTumor Mutational Burden as a Biomarker for Immunotherapy – Clinical Feasibility in NSCLC, Melanoma and Advanced Urothelial CarcinomaCancer Immunotherapy and Biofluid Biopsies 2016 in Boston, USABoston, USASELECTBIOenquiries@selectbiosciences.com

Biomarkers capable of predicting response to checkpoint inhibitor therapies represent a significant clinical need. Increased tumor neo-antigenic burden has been linked to PD1/PD-L1 therapeutic response in several conditions including metastatic melanoma, non-small cell lung carcinoma and microsatellite instable (MSI-H) colorectal cancer (CRC). However, the challenges and high cost associated with neo-antigen discovery has shifted focus towards more efficient methods of response stratification. As such, tumor mutational burden (TMB) determination from comprehensive genomic profiling (CGP) has emerged as a potential solution. Herein, we demonstrate the clinical utility of TMB for predicting response to checkpoint inhibitor blockade across three indications including NSCLC, metastatic melanoma and advanced urothelial carcinoma using the Foundation One platform.


Add to Calendar ▼2016-11-01 00:00:002016-11-02 00:00:00Europe/LondonCancer Immunotherapy and Biofluid Biopsies 2016Cancer Immunotherapy and Biofluid Biopsies 2016 in Boston, USABoston, USASELECTBIOenquiries@selectbiosciences.com